Effects of chum salmon stanniocalcin,a calcium regulatiug hormone in teleosts and its synthetic N-terminal peptide fragment on bone metabolism

Stanniocalcin (STC) from chum salmon (Oncorhynclucs keta) was isolated by extracting the corpuscles of Stannius (CS) with ethanol-ammonium, followed by ion-exchange chromatography, gel filtration and reversed phase high performance liquid chromatography. STC migrated as a 46-kDa product under nonred...

Full description

Bibliographic Details
Main Author: Yoshiko, Yuji
Format: Thesis
Language:English
Published: 2014
Subjects:
490
Online Access:https://ir.lib.hiroshima-u.ac.jp/00031885
https://ir.lib.hiroshima-u.ac.jp/files/public/3/31885/20141016184016628881/diss_otsu2836.pdf
https://doi.org/10.11501/3120004
id fthiroshimauniv:oai:ir.lib.hiroshima-u.ac.jp:00031885
record_format openpolar
institution Open Polar
collection Hiroshima University: Institutional Repository (HiR)
op_collection_id fthiroshimauniv
language English
topic 490
spellingShingle 490
Yoshiko, Yuji
Effects of chum salmon stanniocalcin,a calcium regulatiug hormone in teleosts and its synthetic N-terminal peptide fragment on bone metabolism
topic_facet 490
description Stanniocalcin (STC) from chum salmon (Oncorhynclucs keta) was isolated by extracting the corpuscles of Stannius (CS) with ethanol-ammonium, followed by ion-exchange chromatography, gel filtration and reversed phase high performance liquid chromatography. STC migrated as a 46-kDa product under nonreducing conditions and as a 23-kDa product under reducing conditions on sodium dodecylsulphate-polyacrylamide gel electrophoresis. The protein is likely to be a homodimer composed of two subunits of 23 kDa each. Purified STC decreased the intestinal calcium uptake in a dose related manner in the Atlantic cod (Gadus morhua). A cDNA was cloned from cDNAs of the CS by means of PCR using two primers corresponding to the N- and C-terminal amino acid sequence of STC. Sequence analysis of the protein and the eDNA revealed that chum salmon STC is a homodimer, and that the monomer consists of 179 amino acids including 11 half-Cys residues and one N-linked glycosylation site, which is 44, 52 and 35 residues smaller at the C-terminal region than the sequences deduced from coho salmon, Australian eel and human STC cDNA, respectively. A synthetic peptide (peptide N) corresponding to the N-terminal amino acid residues which had a high amino acid sequence identity with coho salmon and Australian eel STC, was prepared from chum salmon. Its effects were compared with those of intact STC on mammalian bone metabolism in vitro. Peptide N (10-10-10-11 M) slightly decreased the rate of loss of radioactivity from fetal rat calvariae labeled with 45Ca, both with and without stimulation by N-terminal peptide fragment of human parathyroid hormone (hPTH1-34). Intact STC had no effect on the release of 45Ca from the calvariae. Peptide N (10-10-10-12 M) also inhibited increases in the number of tartrate-resistant acid phosphatase-positive multinucleated cells promoted by hPTH1-34 in cultures of murine hemopoietic cells, although intact STC had no effect on the number of the cells. The accumulation of cyclic AMP induced by hPTH 1-34 in ROS 17/2.8-5 cells was suppressed by peptide N (10-10-10-12 M). Peptide N (10- 11-10-13 M) increased the rate of incorporation of [3H]proline into the collagenase-digestible protein of calvariae in newborn mice. These results indicated that the highly conserved amino-terminal region of STC from teleosts has diverse effects on the metabolism of mammalian bone, causing a biphasic response. Such effects have not been observed with materials from the CS and intact STC and they also differ from the effects of hPTH1-34. CONTENTS 1. INTRODUCTION / p1 2. MATERIALS AND METHODS / p4 2.1. Preparation of chum salmon stanniocalcin (STC) / p4 2.2. Intestinal Ca²⁺influx of Atlantic cod / p4 2.3. Preparation of peptide fragments of STC / p5 2.4. Amino acid sequence analysis / p5 2.5. Cloning of cDNA encoding STC / p6 2.6. Synthesis of N-terminal peptide fragment of STC (peptide N) / p7 2.7. Calvarial bone resorption assay / p7 2.8. Generation of osteoclast-like cells / p8 2.9. Production of cyclic AMP in osteoblast-like cells / p8 2.10. Synthesis of collagen in calvarial bone / p9 2.11. Statistical analysis / p9 3. RESULTS / p10 3.1. Isolation and characterization of STC / p10 3.2. Amino acid and cDNA sequence analysis of STC / p11 3.3. Synthesis of peptide N / p12 3.4. Effects of STC and peptide N on the calvarial bone resorption / p12 3.5. Effects of STC and peptide N on generation of osteoclast-like cells / p13 3.6. Effects of peptide N on the production of cyclic AMP in osteoblast-like cells / p14 3.7. Effects of peptide N on the synthesis of calvarial bone collagen / p14 4. DISCUSSION / p16 4.1. Chemical properties of STC / p16 4.2. Effects of STC and peptide N on the metabolism of mammalian bone / p18 5. SUMMARY / p23 6. REFERENCES / p25 広島大学(Hiroshima University) 博士(歯学) Dentistry doctoral
format Thesis
author Yoshiko, Yuji
author_facet Yoshiko, Yuji
author_sort Yoshiko, Yuji
title Effects of chum salmon stanniocalcin,a calcium regulatiug hormone in teleosts and its synthetic N-terminal peptide fragment on bone metabolism
title_short Effects of chum salmon stanniocalcin,a calcium regulatiug hormone in teleosts and its synthetic N-terminal peptide fragment on bone metabolism
title_full Effects of chum salmon stanniocalcin,a calcium regulatiug hormone in teleosts and its synthetic N-terminal peptide fragment on bone metabolism
title_fullStr Effects of chum salmon stanniocalcin,a calcium regulatiug hormone in teleosts and its synthetic N-terminal peptide fragment on bone metabolism
title_full_unstemmed Effects of chum salmon stanniocalcin,a calcium regulatiug hormone in teleosts and its synthetic N-terminal peptide fragment on bone metabolism
title_sort effects of chum salmon stanniocalcin,a calcium regulatiug hormone in teleosts and its synthetic n-terminal peptide fragment on bone metabolism
publishDate 2014
url https://ir.lib.hiroshima-u.ac.jp/00031885
https://ir.lib.hiroshima-u.ac.jp/files/public/3/31885/20141016184016628881/diss_otsu2836.pdf
https://doi.org/10.11501/3120004
long_lat ENVELOPE(-19.455,-19.455,65.656,65.656)
geographic Keta
geographic_facet Keta
genre atlantic cod
Gadus morhua
genre_facet atlantic cod
Gadus morhua
op_relation Yoshiko, Y., Kosugi, T. and Koide, Y. Effects of a synthetic N-terminal fragment of stanniocalcin on the metabolism of mammalian bone in vitro. Biochimica et Biophysica Acta, in press.
http://dx.doi.org/10.1016/0167-4889(95)00160-3
https://ir.lib.hiroshima-u.ac.jp/files/public/3/31885/20141016184016628881/diss_otsu2836.pdf
http://doi.org/10.11501/3120004
15401乙第2836号
https://ir.lib.hiroshima-u.ac.jp/00031885
op_rights Copyright(c) by Author
op_doi https://doi.org/10.11501/3120004
https://doi.org/10.1016/0167-4889(95)00160-3
_version_ 1766358239704776704
spelling fthiroshimauniv:oai:ir.lib.hiroshima-u.ac.jp:00031885 2023-05-15T15:27:50+02:00 Effects of chum salmon stanniocalcin,a calcium regulatiug hormone in teleosts and its synthetic N-terminal peptide fragment on bone metabolism 硬骨魚類由来カルシウム代謝調節ホルモン・スタニオカルシンの骨代謝調節作用 Yoshiko, Yuji 2014-10-17 application/pdf https://ir.lib.hiroshima-u.ac.jp/00031885 https://ir.lib.hiroshima-u.ac.jp/files/public/3/31885/20141016184016628881/diss_otsu2836.pdf https://doi.org/10.11501/3120004 eng eng Yoshiko, Y., Kosugi, T. and Koide, Y. Effects of a synthetic N-terminal fragment of stanniocalcin on the metabolism of mammalian bone in vitro. Biochimica et Biophysica Acta, in press. http://dx.doi.org/10.1016/0167-4889(95)00160-3 https://ir.lib.hiroshima-u.ac.jp/files/public/3/31885/20141016184016628881/diss_otsu2836.pdf http://doi.org/10.11501/3120004 15401乙第2836号 https://ir.lib.hiroshima-u.ac.jp/00031885 Copyright(c) by Author 490 Thesis or Dissertation text 2014 fthiroshimauniv https://doi.org/10.11501/3120004 https://doi.org/10.1016/0167-4889(95)00160-3 2020-12-23T23:26:58Z Stanniocalcin (STC) from chum salmon (Oncorhynclucs keta) was isolated by extracting the corpuscles of Stannius (CS) with ethanol-ammonium, followed by ion-exchange chromatography, gel filtration and reversed phase high performance liquid chromatography. STC migrated as a 46-kDa product under nonreducing conditions and as a 23-kDa product under reducing conditions on sodium dodecylsulphate-polyacrylamide gel electrophoresis. The protein is likely to be a homodimer composed of two subunits of 23 kDa each. Purified STC decreased the intestinal calcium uptake in a dose related manner in the Atlantic cod (Gadus morhua). A cDNA was cloned from cDNAs of the CS by means of PCR using two primers corresponding to the N- and C-terminal amino acid sequence of STC. Sequence analysis of the protein and the eDNA revealed that chum salmon STC is a homodimer, and that the monomer consists of 179 amino acids including 11 half-Cys residues and one N-linked glycosylation site, which is 44, 52 and 35 residues smaller at the C-terminal region than the sequences deduced from coho salmon, Australian eel and human STC cDNA, respectively. A synthetic peptide (peptide N) corresponding to the N-terminal amino acid residues which had a high amino acid sequence identity with coho salmon and Australian eel STC, was prepared from chum salmon. Its effects were compared with those of intact STC on mammalian bone metabolism in vitro. Peptide N (10-10-10-11 M) slightly decreased the rate of loss of radioactivity from fetal rat calvariae labeled with 45Ca, both with and without stimulation by N-terminal peptide fragment of human parathyroid hormone (hPTH1-34). Intact STC had no effect on the release of 45Ca from the calvariae. Peptide N (10-10-10-12 M) also inhibited increases in the number of tartrate-resistant acid phosphatase-positive multinucleated cells promoted by hPTH1-34 in cultures of murine hemopoietic cells, although intact STC had no effect on the number of the cells. The accumulation of cyclic AMP induced by hPTH 1-34 in ROS 17/2.8-5 cells was suppressed by peptide N (10-10-10-12 M). Peptide N (10- 11-10-13 M) increased the rate of incorporation of [3H]proline into the collagenase-digestible protein of calvariae in newborn mice. These results indicated that the highly conserved amino-terminal region of STC from teleosts has diverse effects on the metabolism of mammalian bone, causing a biphasic response. Such effects have not been observed with materials from the CS and intact STC and they also differ from the effects of hPTH1-34. CONTENTS 1. INTRODUCTION / p1 2. MATERIALS AND METHODS / p4 2.1. Preparation of chum salmon stanniocalcin (STC) / p4 2.2. Intestinal Ca²⁺influx of Atlantic cod / p4 2.3. Preparation of peptide fragments of STC / p5 2.4. Amino acid sequence analysis / p5 2.5. Cloning of cDNA encoding STC / p6 2.6. Synthesis of N-terminal peptide fragment of STC (peptide N) / p7 2.7. Calvarial bone resorption assay / p7 2.8. Generation of osteoclast-like cells / p8 2.9. Production of cyclic AMP in osteoblast-like cells / p8 2.10. Synthesis of collagen in calvarial bone / p9 2.11. Statistical analysis / p9 3. RESULTS / p10 3.1. Isolation and characterization of STC / p10 3.2. Amino acid and cDNA sequence analysis of STC / p11 3.3. Synthesis of peptide N / p12 3.4. Effects of STC and peptide N on the calvarial bone resorption / p12 3.5. Effects of STC and peptide N on generation of osteoclast-like cells / p13 3.6. Effects of peptide N on the production of cyclic AMP in osteoblast-like cells / p14 3.7. Effects of peptide N on the synthesis of calvarial bone collagen / p14 4. DISCUSSION / p16 4.1. Chemical properties of STC / p16 4.2. Effects of STC and peptide N on the metabolism of mammalian bone / p18 5. SUMMARY / p23 6. REFERENCES / p25 広島大学(Hiroshima University) 博士(歯学) Dentistry doctoral Thesis atlantic cod Gadus morhua Hiroshima University: Institutional Repository (HiR) Keta ENVELOPE(-19.455,-19.455,65.656,65.656)